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Tramadol Induced Adrenal Insufficiency: Histological Immunohistochemical Ultrastructural and Biochemical Genetic Experimental Study

机译:曲马多引起的肾上腺功能不全:组织学免疫组化超微结构和生化遗传实验研究

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摘要

Tramadol is a synthetic, centrally acting analgesic. It is the most consumed narcotic drug that is prescribed in the world. Tramadol abuse has dramatically increased in Egypt. Long term use of tramadol can induce endocrinopathy. So, the aim of this study was to analyze the adrenal insufficiency induced by long term use of tramadol in experimental animals and also to assess its withdrawal effects through histopathological and biochemical genetic study. Forty male albino rats were used in this study. The rats were divided into 4 groups (control group, tramadol-treated group, and withdrawal groups). Tramadol was given to albino rats at a dose of 80 mg/kg body weight for 3 months and after withdrawal periods (7–15 days) rats were sacrificed. Long term use of tramadol induced severe histopathological changes in adrenal glands. Tramadol decreased the levels of serum cortisol and DHEAS hormones. In addition, it increased the level of adrenal MDA and decreased the genetic expression of glutathione peroxidase and thioredoxin reductase in adrenal gland tissues. All these changes started to return to normal after withdrawal of tramadol. Thus, it was confirmed that long term use of tramadol can induce severe adrenal insufficiency.
机译:曲马多是一种合成的中枢镇痛药。它是世界上处方最消耗的麻醉药品。曲马多的滥用在埃及急剧增加。长期使用曲马多会诱发内分泌病。因此,本研究的目的是分析长期服用曲马多引起的肾上腺功能不全,并通过组织病理学和生化遗传研究评估其戒断作用。在该研究中使用了40只雄性白化病大鼠。将大鼠分为4组(对照组,曲马多治疗组和戒断组)。将曲马多以80微克/千克体重的剂量给予白化病大鼠3个月,停药期(7-15天)后处死大鼠。长期使用曲马多会引起肾上腺的严重组织病理学改变。曲马多降低血清皮质醇和DHEAS激素的水平。另外,它增加了肾上腺组织中的肾上腺MDA水平并降低了谷胱甘肽过氧化物酶和硫氧还蛋白还原酶的基因表达。撤出曲马多后,所有这些变化开始恢复正常。因此,证实了长期使用曲马多会引起严重的肾上腺功能不全。

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